NDC 71335-1572 – Pantoprazole Sodium

Pantoprazole Sodium 20 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-1572

Product details

Brand name
Pantoprazole Sodium
Generic name
Pantoprazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202882
Marketed since
September 10, 2014
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pantoprazole Sodium →

Package NDC codes (9)

Package NDCDescriptionSince
71335-1572-160 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-1)Apr 23, 2020
71335-1572-230 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-2)May 29, 2020
71335-1572-390 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-3)Apr 21, 2020
71335-1572-456 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-4)May 13, 2026
71335-1572-528 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-5)May 13, 2026
71335-1572-610 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-6)May 13, 2026
71335-1572-7120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-7)May 13, 2026
71335-1572-8180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-8)Jul 7, 2020
71335-1572-93 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-9)May 13, 2026

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